| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:48617791-48618071 | Common:1; Rare:80 | ||||
| chr19:48619136-48619667 | Common:1; Rare:165 | ||||
| chr19:48624050-48624417 | Common:1; Rare:89 | ||||
| chr19:48645996-48646226 | Rare:33 | ||||
| chr19:48810979-48811264 | Rare:86 | ||||
| chr19:48868179-48868711 | Common:2; Rare:94 | ||||
| chr19:48872218-48872823 | Common:5; Rare:180 | ||||
| chr19:48874698-48875313 | Common:10; Rare:192 | ||||
| chr19:48955132-48955730 | Common:3; Rare:150; Clinvar (pathogenic):1 | ||||
| chr19:48955822-48955847 | Rare:7 | ||||
| chr19:48965229-48965440 | Rare:64; Clinvar:1; Clinvar (pathogenic):5 | ||||
| chr19:48965538-48965915 | Common:1; Rare:139; Clinvar:4; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr19:48993200-48993584 | Common:4; Rare:166; Clinvar:3; Clinvar (benign):3 | ||||
| chr19:48993840-48993912 | Common:3; Rare:28 | ||||
| chr19:49085090-49085629 | Common:3; Rare:204 |